Sentence examples for mutation in mitochondrial from inspiring English sources

Galmiche, L. et al. Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy.

It seems that every few thousand years or so, a harmless mutation in mitochondrial DNA passes to succeeding generations; each becomes a distinctive mark of common ancestry.

Ikawa, M. et al. Evaluation of Systemic Redox States in Patients Carrying the MELAS A3243G Mutation in Mitochondrial DNA.

To report the histopathologic findings of eyes from a patient with Leigh's syndrome associated with the T 8993-G point mutation in mitochondrial DNA (mtDNA).

Moreover, the imported oligoribonucleotide designed to target a pathogenic point mutation in mitochondrial DNA was able to induce a decrease in the proportion of mutant mitochondrial genomes.

The current version of the hearing loss biochip detects nine common mutations in the connexin 26 gene, four mutations in the pendrin gene, one mutation in the usherin gene, and one mutation in mitochondrial DNA.

Three mutations that had no discernable effect on Y. lipolytica complex I, R147W, R199P and A341V, were heterozygous plus a mutation in mitochondrial-encoded ND5 (25), compound heterozygous with R88G (24) and homozygous (30, 40), respectively (Table 1).

One study follows mutations in mitochondrial DNA (the female lineage), the second follows Y chromosome changes (the male lineage).

Harmful mutations in mitochondrial DNA cause progressive and often fatal diseases that typically affect the heart, brain and muscles.

Harmful mutations in mitochondrial DNA can have a devastating impact on children who inherit them.

Mutations in mitochondrial DNA (mtDNA) are a common cause of genetic disease.